Content Clearance Lead
About The Position
We are looking for a Content Clearance Lead who is intellectually curious, self-driven, and adaptable to join our the Omnichannel and Content Operations team based in our Atlanta, Georgia office in the United States. This hybrid position requires a minimum of 40% on site presence and up to 10% domestic/international travel. About the role You will serve as the US business partner for the content clearance process (Review Committee or Medical-Legal-Regulatory Review) consisting of promotional and non-promotional materials. The Lead manages the review, discussion and approval of content, materials, and initiatives, with application and interpretation of regulations and industry guidance. Who you’ll work with You will work with Regulatory, Legal, Compliance, Medical Leads, Marketing Leads, Market Access, Patient Value Units, as well as all cross functional Subject Matter Experts and stakeholders that have input into the strategy and creation of promotional and non-promotional material.
Requirements
- Bachelor’s degree
- 5+ years of experience in pharmaceutical industry or life sciences industry, preferably in controlled process environment including development and approval of regulated information and materials.
- Intermediate to advanced knowledge of US regulations for the promotion of pharmaceutical and biological products with proficiency in identifying emerging issues and making recommendations for resolution.
- Ability to support multiple products or indications in all lifecycle stages; interpret and apply strategic business objectives to the clearance and ad/promo domain.
- Excellent organization, time management, planning, and prioritization skills, with attention to detail.
- Proven ability to work collaboratively and with sensitivity in a matrix organization.
- Demonstrated aptitude for producing clear, concise verbal and written communications
Responsibilities
- Perform initial quality reviews of materials and route submissions per internal governance standards.
- Act as a Chair for Clearance Committees and lead efficient, effective content review meetings.
- Partner with stakeholders to define project timelines, manage priorities, and advise on content processes.
- Forecast review demand and manage approvals across planning, review, health authority submissions, dissemination and withdrawal lifecycle stages.
- Ensure compliance with UCB standards and U.S. promotional labeling regulations.
- Drive continuous improvement through retrospectives, deviation tracking, and root cause analysis.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
1,001-5,000 employees
